PMC Links for Nucleotide (Select 224282158) - PMC

Select item 13775011.

A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

W Ahmad, A D Irvine, H Lam, C Buckley, E A Bingham, A A Panteleyev, M Ahmad, J A McGrath, A M Christiano

Am J Hum Genet. 1998 Oct; 63(4): 984–991. doi: 10.1086/302069

PMCID:: PMC1377501

Summary PDF–979K

Select item 13768932.

A gene for universal congenital alopecia maps to chromosome 8p21-22.

M M Nöthen, S Cichon, I R Vogt, S Hemmer, R Kruse, M Knapp, T Höller, M Faiyaz ul Haque, S Haque, P Propping, M Ahmad, M Rietschel

Am J Hum Genet. 1998 Feb; 62(2): 386–390. doi: 10.1086/301717

PMCID:: PMC1376893

Summary PDF–255K

Select item 53649653.

Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis

Feng-Tao Shi, Mei Yu, David Zloty, Robert H. Bell, Eddy Wang, Noushin Akhoundsadegh, Gigi Leung, Anne Haegert, Nicholas Carr, Jerry Shapiro, Kevin J. McElwee

Mol Med Rep. 2017 Apr; 15(4): 1441–1454. Published online 2017 Feb 2. doi: 10.3892/mmr.2017.6163

PMCID:: PMC5364965

Article PDF–1.3M

Select item 50869884.

Notch3 drives development and progression of cholangiocarcinoma

Rachel V. Guest, Luke Boulter, Benjamin J. Dwyer, Timothy J. Kendall, Tak-Yung Man, Sarah E. Minnis-Lyons, Wei-Yu Lu, Andrew J. Robson, Sofia Ferreira Gonzalez, Alexander Raven, Davina Wojtacha, Jennifer P. Morton, Mina Komuta, Tania Roskams, Stephen J. Wigmore, Owen J. Sansom, Stuart J. Forbes

Proc Natl Acad Sci U S A. 2016 Oct 25; 113(43): 12250–12255. Published online 2016 Oct 10. doi: 10.1073/pnas.1600067113

PMCID:: PMC5086988

Article PDF–1.5M

Select item 33596125.

Notch1 Is Regulated by Chorionic Gonadotropin and Progesterone in Endometrial Stromal Cells and Modulates Decidualization in Primates

Yalda Afshar, Lucio Miele, Asgerally T. Fazleabas

Endocrinology. 2012 Jun; 153(6): 2884–2896. Published online 2012 Apr 24. doi: 10.1210/en.2011-2122

PMCID:: PMC3359612

Article

Select item 27473276.

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, Muhammad Jawad Hassan, Muhammad Ansar, Wasim Ahmad, Suzanne M Leal

J Hum Genet. Author manuscript; available in PMC 2009 Sep 21.

Published in final edited form as: J Hum Genet. 2009 Mar; 54(3): 141–144. Published online 2009 Feb 20. doi: 10.1038/jhg.2009.2

PMCID:: PMC2747327

Article PDF–315K

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